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References in periodicals archive ?
Newborn twins with thrombocytopenia, coagulation defects, and hepatosplenomegaly.
It showed massive hepatosplenomegaly with multiple splenic infarctions (Fig.
Ultrasonography of the abdomen revealed hepatosplenomegaly, with liver measuring 16.
Anemia with hepatosplenomegaly is a common presentation of hemolytic anemia in infancy.
5,6) T-PLL is characterized by marked leukocytosis, lymphadenopathy, hepatosplenomegaly, and cutaneous involvement, which occur in about a quarter of patients.
2,3) Due to immune complex mediated damage there can also be lymphadenitis, neuritis, iridocyclitis, arthritis, synovitis, myositis, epididymo-orchitis, glomerulonephritis and involvement of the liver and spleen leading to hepatosplenomegaly.
1) It is characterized by a primary extranodal involvement of medium-sized lymphoid cells, typically with sinusoidal infiltration of the liver, spleen, and bone marrow, which results in hepatosplenomegaly, peripheral blood cytopenias, and other related systemic symptoms.
It is characterized by persistent fever, pancytopenia, liver dysfunction, hepatosplenomegaly, hyperferritinemia, hypofibrinogenemia, elevated serum lactate dehydrogenase, and hypertriglyceridemia.
Physical examination showed hepatosplenomegaly multiple hypopigmentation on face and extremities bluish iris and silver hair.
1 HLH represents a severe hyper-inflammatory condition with the cardinal symptoms of prolonged fever, cytopenias, hepatosplenomegaly, and hemophagocytosis by activated, morphologically benign macrophages.
While being investigated she developed a sepsis like picture with fever, petechial hemorrhages and hepatosplenomegaly.